potassium chloride extended-release (50090-7192)

Drug Facts

Product Profile

Brand Name potassium chloride extended-release

Generic Name potassium chloride extended-release

Labeler a-s medication solutions

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

potassium chloride 1500 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7192

Product ID 50090-7192_a8b0a12a-70d2-4ea7-92cf-65b65b8ad7d5

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA214452

Listing Expiration 2026-12-31

Marketing Start 2021-01-30

Pharmacologic Class

Classes

increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907192

Hyphenated Format 50090-7192

Supplemental Identifiers

RxCUI

1801294

UNII

660YQ98I10

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride extended-release (source: ndc)

Generic Name potassium chloride extended-release (source: ndc)

Application Number ANDA214452 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

1500 mg/1

source: ndc

Packaging

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-0)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-1)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-2)

source: ndc

Packages (3)

50090-7192-0 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-0) 50090-7192-1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-1) 50090-7192-2 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-2)

Ingredients (1)

potassium chloride (1500 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "a8b0a12a-70d2-4ea7-92cf-65b65b8ad7d5", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["de335131-bb8a-44e5-89fa-1478edbcdc0e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-0)", "package_ndc": "50090-7192-0", "marketing_start_date": "20240717"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-1)", "package_ndc": "50090-7192-1", "marketing_start_date": "20240717"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7192-2)", "package_ndc": "50090-7192-2", "marketing_start_date": "20240717"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "50090-7192_a8b0a12a-70d2-4ea7-92cf-65b65b8ad7d5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "50090-7192", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}